期刊
FUEL
卷 321, 期 -, 页码 -出版社
ELSEVIER SCI LTD
DOI: 10.1016/j.fuel.2022.123980
关键词
Ethanol; Dehydrogenation; Acetaldehyde; Hydrogen; Hydrotalcite
资金
- National Natural Science Foundation of China [21773206, 21473155]
- Natural Science Foundation of Zhejiang Province [LZ12B03001]
In this study, a catalyst with abundant Cu sites and strong metal-support interaction was synthesized through controlled calcination and reduction. The catalyst demonstrated excellent activity and selectivity for the dehydrogenation of ethanol to acetaldehyde, and maintained its activity for a prolonged period of time.
Ethanol is one of the most promising bio-based renewable platform chemicals. Catalytic upgrading of ethanol into valuable products is of great importance, and co-production of hydrogen and acetaldehyde via the dehydrogenation of ethanol is an effective way for its high atomic utilization. In this work, unsaturated Cu sites (Cu-1.4/ZnxMg4.6-xAl2O7.6) with plenty interface of between Cu and support, strong metal-support interaction were synthesized via the controlled calcination and reduction of hydrotalcite-like Cu1.4ZnxMg4.6-xAl2(OH)(16)CO3 and used in the dehydrogenation of ethanol. Characterization results disclosed that the dispersion of Cu and surface area of Cu-1.4/Zn3.2Mg1.4Al2O7.6 reached 77.8% and 167.5 m(2)/g, respectively. This catalyst exhibited excellent activity for the dehydrogenation of ethanol to acetaldehyde, and the detected selectivity of acetaldehyde and H-2 was higher than 98.5% at 280 degrees C, 0.1 MPa and WHSV = 11.8 h(-1). The calculated space-time yield of acetaldehyde reached 7.0 g-acetaldehyde/g-cat/h. At the same time, Cu-1.4/Zn3.2Mg1.4Al2O7.6 could maintain its activity within 50 h on stream.
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